RIVA, PAOLA VANDA
RIVA, PAOLA VANDA
Dipartimento di Biotecnologie Mediche e Medicina Traslazionale
19p deletion in recurring leiomyosarcoma lesions from the same patient
2000 P. Riva, L. Dalprá, V. Gualandri, M. Volontè, M. Miozzo, R. Malgara, A. F. Conti, L. Larizza
1p36 LOH and expression study of apoptotic genes in a selected group of chordomas
2006 M. Longoni, F. Orzan, M. Stroppi, N. Boari, P. Mortini, P. Riva
A 12-bp deletion (7818del12) in the c-kit protooncogene in a large Italian kindred with piebaldism
1995 P. Riva, N. Milani, P. Gandolfi, L. Larizza
A novel potentially diagnostic polymorphism (4894 A/C) in exon 10 of the human c-kit proto-oncogene
1996 P. Riva, L. Larizza
A tandem duplication of chromosome 21 in a newborn showing a phenotype inconsistent with Down syndrome
2010 E. Martinoli, G.V. Zuccotti, L. Pogliani, M. Volontè, M. Venturin, P. Fortina, A. Ertel, S. Redaelli, P.V. Riva, L. Dalprà
A Translational Approach to Spinal Neurofibromatosis: Clinical and Molecular Insights from a Wide Italian Cohort
2023 R. Paterra, P. Bettinaglio, A. Borghi, E. Mangano, V. Tritto, C. Cesaretti, C. Schettino, R. Bordoni, C. Santoro, S. Avignone, M.E.M. Moscatelli, M. Anna Beatrice Melone, V. Saletti, G. Piluso, F. Natacci, P.V. Riva, M. Eoli
A tumor suppressor locus in familial and sporadic chordoma maps to 1p36
2000 M. Miozzo, L. Dalprà, P. Riva, M. Volontè, F. Macciardi, S. Pericotti, M. G. Tibiletti, M. Cerati, K. Rohde, L. Larizza, A. M. Fuhrman Conti
ADAP2 in heart development: a candidate gene for the occurrence of cardiovascular malformations in NF1 microdeletion syndrome
2014 M. Venturin, S. Carra, G. Gaudenzi, S. Brunelli, G.R. Gallo, S. Moncini, F. Cotelli, P. Riva
Breakpoint characterization of a novel NF1 multiexonic deletion : a case showing expression of the mutated allele
2008 F. Orzan, M. Stroppi, M. Venturin, M.C. Valero, C. Hernández, P. Riva
Centa2 is expressed during heart development and is a candidate gene for CVMs
2008 M. Venturin, S. Brunelli, G. Gaudenzi, M. Stroppi, M. Crippa, F. Cotelli, P. Riva
Centa2 è espresso durante lo sviluppo del cuore ed è un gene candidato per le malformazioni cardiovascolari
2008 M. Venturin, M. Stroppi, S. Brunelli, G. Gaudenzi, F. Cotelli, P. Riva
Centaurin-α2 and tubulin interaction increases microtubule stability
2010 M. Stroppi, D. Cartelli, G. Cappelletti, M. Venturin, S. Rigoletto, E. Battaglioli, P. Riva
Centaurin-α2 Interacts with β-Tubulin and Stabilizes Microtubules
2012 P. Zuccotti, D. Cartelli, M. Stroppi, V. Pandini, M. Venturin, A. Aliverti, E. Battaglioli, G. Cappelletti, P.V. Riva
Changes of RAS Pathway Phosphorylation in Lymphoblastoid Cell Lines from Noonan Syndrome Patients Carrying Hypomorphic Variants in Two NS Genes
2023 V. Tritto, D. Capitanio, C. Gelfi, P. Riva
Characterization of 22q12 Microdeletions Causing Position Effect in Rare NF2 Patients with Complex Phenotypes
2022 V. Tritto, M. Eoli, R. Paterra, S. Redaelli, M. Moscatelli, F. Rusconi, P. Riva
Characterization of a cytogenetic 17q11.2 deletion in an NF1 patient with a contiguous gene syndrome
1996 P. Riva, P. Castorina, S. Manoukian, L. Dalprà, L. Doneda, G. Marini, J. den Dunnen, L. Larizza
Characterization of a non-recurrent familial translocation t(7;9)(q11.23;p24.3) points to a recurrent involvement of the Williams-Beuren syndrome region in chromosomal rearrangements
2006 G. Portera, M. Venturin, A. Patrizi, E. Martinoli, P. Riva, L. Dalprà
Characterization of breakpoint boundaries in 19 Neurofibromatosis type 1 microdeletions
2005 C. Gervasini, M. Venturin, F. Orzan, R. Tenconi, M. Upadhyaya, P. Riva, L. Larizza
Chromosomal instability in Cancer : a genomic condition reflecting alterations of different cellular mechanisms
2008 P. Riva, M. Longoni
Chromosomal instability in fibroblasts and mesenchymal tumors from 2 sibs with Rothmund-Thomson syndrome
1998 M. Miozzo, P. Castorina, P. Riva, L. Dalprà, A. M. Fuhrman Conti, L. Volpi, T. S. Hoe, A. Khoo, J. Wiegant, C. Rosenberg, L. Larizza